Intracellular reactive apoptosis and reactive oxygen species (ROS) play a crucial role in ultraviolet- (UV-) induced inflammation and aging reaction in human dermal tissues. This study determines the mechanism by which Haematococcus pluvialis extracts (HPE) and purified astaxanthin (HPA) to promote skin regeneration in the injured tissue in vitro and in vivo. The results show that HPE and HPA decrease the DNA damage and promote the secretion of collagen from the human normal fibroblast cell line (Hs68) in a dose-dependent manner. UV irradiation and HPA reduce oxidative stress damage due to phorbol-12-myristate-13-acetate (PMA). When skin cells are injured by free radicals, cells undergo a programmed cellular death. Cellular apoptotic death is determined using annexin V-fluorescein isothiocyanate (FITC)/propidium iodide (PI) double staining to verify that there is no cell membrane asymmetry and that the nuclear membrane is broken. Inflammatory symptoms and apoptotic injuries to experimental rats in a group that is treated with HPA treated are decreased in a dose-dependent manner after UVB exposure (300 mJ/cm²) for 15 min in vivo, compared to the vehicle control group. These positive results show that HPA repairs UVB-triggered skin tissue injury and aging by conducting electrons out of cells to maintain a low level of oxidative stress so that collagen is synthesized in vitro and in vivo.

In this research we utilized extracts from two different nature products, Achatina fulica and Heimiella retispora, to enhance skin moisturizing abilities, anti-oxidative properties, and cell proliferations. It was observed that two polysaccharides with anti-oxidative effects by chelating metal ions reduced oxidative stress and further blocked the formation of reactive oxygen species syntheses. To detect whether there was a similar effect within the cellular mechanism, a flow cytometry was applied for sensing the oxidative level and it was found that both materials inhibited the endogenous oxidative stress, which was induced by phorbol-12-myristate-13-acetate (PMA). Both polysaccharides also stimulated the production of collagen to maintain skin tightness and a moisturizing effect. In summary, we developed two macromolecular polysaccharides with potential applications in dermal care.

This paper emphasizes that the furnace pressure, crucible rotation, and pulling rate have important effects on interstitial oxygen (O_i) concentrations and micro-defects during growth in a Czochralski single-crystal silicon (CZ-Si) growth furnace. Since oxygen in a silicon ingot influences minority carrier lifetime, different set-points of furnace pressure and crucible rotation were controlled to achieve different degrees of O_i. The O_i content has a positive correlation with furnace pressure and crucible rotation. Various numbers of micro-defects were generated under the influence of different pulling rates, owing to the transformation from liquid to solid. The sample also underwent Secco etching and a high-temperature wet oxidation to observe defects caused by the O_i concentration and pulling rate, namely, flow pattern defects (FPDs) and oxidation-induced stacking faults (OISFs). Optical microscopy was employed to confirm the surface topography, and for defect number counting, to observe the correlation between the defects and the minority carrier lifetime. The overall results show that the minority carrier lifetime is mainly dominated by OISFs under high O_i content and FPDs under low O_i content. Therefore, growth using a CZ-Si growth furnace should be carried out with low furnace pressure, low crucible rotation, and low pulling rate to reduce micro-defects.

There are many compounds used to treat cancer, but still, only 20% of proposed anticancer agents have been commercialized after clinical trials due to serious side effects and unsatisfactory results. To screen potential drugs precisely and quickly, this study develops a flexible bioimpedance sensor. The sensor positively detects the half maximal inhibitory concentration (IC50) of drugs in real time by analyzing phase angle changes during cell mortality. The best results are achieved using a probe separation of A12B34 at logarithmic frequencies of 163 Hz and 77.87 kHz. At these two frequencies, there is a linear relationship with the phase angle at 0% and 50% of the dead cells. Dividing the phase angle at the two frequencies shows a 17.98% change in the phase angle, which allows self-correction and insensitivity to the number of cells. A custom phase angle measurement device is developed for detection at 163 Hz and 77.87 kHz, respectively. This study develops a novel sensor that is precise and fast and allows high-throughput analysis to detect the inhibition of cancer in real time. This sensor is an alternative to traditional chemical detection methods because it is faster, cheaper, and more accurate.

Breath ammonia is recognized as a potential non-invasive biomarker for renal function assessment. In this study, we applied our previously developed Tin oxide (SnO₂) gas sensing technology—to a new clinical application: real-time monitoring of exhaled ammonia in hemodialysis (HD) patients. The SnO₂ membrane gas sensor exhibited high sensitivity, low detection limit, and excellent selectivity toward ammonia due to the synergistic effects of SnO₂ membrane. A total of 88 HD patients were recruited, and breath samples were collected immediately before and after dialysis. Results showed a significant decrease in breath ammonia concentration post-dialysis (56.02 ± 65.72 ppm to 33.13 ± 39.57 ppm, p = 0.0021). No significant correlations were found between ammonia changes and conventional dialysis indicators (Kt/V, URR, nPCR), likely due to sampling time variability and calibration differences. This work demonstrates the potential medical application of a SnO₂-based gas sensing platform, providing a rapid and non-invasive approach that may be relevant to bedside dialysis monitoring.